Филогенетическая и онтогенетическая роль плацентарной децидуальной оболочки в становлении и особенностях течения беременности

1. Diessler M.E., Hernández R., Gomez Castro G., Barbeito C.G. Decidual cells and decidualization in the carnivoran endotheliochorial placenta. Front. Cell Dev. Biol. 2023; 16(11):1134874. https://dx.doi.org/10.3389/fcell.2023.1134874
2. Foster C.S.P., Van Dyke J.U., Thompson M.B., Smith N.M.A., Simpfendorfer C.A., Murphy C.R. et al. Different genes are recruited during convergent evolution of pregnancy and the placenta. Mol. Biol. Evol. 2022; 39(4): msac077. https://dx.doi.org/10.1093/molbev/msac077
3. Li L., Feng T., Zhou W., Liu Y., Li H. miRNAs in decidual NK cells: regulators worthy of attention during pregnancy. Reprod. Biol. Endocrinol. 2021; 19(1): 150. https://dx.doi.org/10.1186/s12958-021-00812-2
4. Jing T., Shijian Lv., Jieqiong Y., Li H., Li W., Zhang C. Decidualization and related pregnancy complications. Maternal-Fetal Medicine. 2022; 4(1): 24-35. https://dx.doi.org/10.1097/FM9.0000000000000135
5. Murata H., Tanaka S., Okada H. Immune tolerance of the human decidua. J. Clin. Med. 2021; 10(2): 351. https://dx.doi.org/10.3390/jcm10020351
6. Sun F., Wang S., Du M. Functional regulation of decidual macrophages duringpregnancy. J. Reprod. Immunol. 2021; 143: 103264. https://dx.doi.org/10.1016/j.jri.2020.103264
7. Zhao H., Wong R.J., Stevenson D.K. The impact of hypoxia in early pregnancy on placental cells. Int. J. Mol. Sci. 2021; 22(18): 9675. https://dx.doi.org/10.3390/ijms22189675
8. Ning F., Liu H., Lash G.E. The role of decidual macrophages during normal and pathological pregnancy. Am. J. Reprod. Immunol. 2016; 75(3): 298-309. https://dx.doi.org/10.1111/aji.12477
9. Jarrell J. The significance and evolution of menstruation. Best Pract. Res. Clin. Obstet. Gynaecol. 2018; 50: 18-26. https://dx.doi.org/10.1016/j.bpobgyn.2018.01.007
10. Липатов И.С., Тезиков Ю.В., Кутузова О.А., Приходько А.В., Фролова Н.А., Рябова С.А. Клинико-патогенетические варианты дезадаптации беременных на ранних сроках гестации. Акушерство, гинекология и репродукция. 2017; 11(1): 5-13.
11. Diakiw S.M., Hall J.M.M., Ver Milyea M., Lim A.Y.X., Quangkananurug W., Chanchamroen S. et al. An artificial intelligence model correlated with morphological and genetic features of blastocyst quality improves ranking of viable embryos. Reprod. Biomed. Online. 2022; 45(6): 1105-17. https://dx.doi.org/10.1016/j.rbmo.2022.07.018
12. Bezemer R.E., Faas M.M., van Goor H., Gordijn S.J., Prins J.R. Decidual macrophages and Hofbauer cells in fetal growth restriction. Front. Immunol. 2024; 28(15):1379537. https://dx.doi.org/10.3389/fimmu.2024.1379537
13. Bezemer R.E., Schoots M.H., Timmer A., Scherjon S.A., Erwich J.J.H.M., van Goor H. et al. Altered levels of decidual immune cell subsets in fetal growth restriction, stillbirth, and placental pathology. Front. Immunol. 2020; 20(11): 1898. https://dx.doi.org/10.3389/fimmu.2020.01898
14. Roberts R.M., Green J.A., Schulz L.C. The evolution of the placenta. Reproduction. 2016; 152(5): R179-89. https://dx.doi.org/10.1530/REP-16-0325
15. Booker W., Moroz L. Abnormal placentation. Semin. Perinatol. 2019; 43(1): 51-9. https://dx.doi.org/10.1053/j.semperi.2018.11.009.
16. Ant L., Dily F.L., Beato M., Saragüeta P. Quantitative analysis of cellular morphology during in vitro decidualization. Curr. Protoc. 2023; 3(10): e895. https://dx.doi.org/10.1002/cpz1.895
17. Carter A.M. Genomics, the diversification of mammals, and the evolution of placentation. Dev. Biol. 2024; 516: 167-82. https://dx.doi.org/10.1016/j.ydbio.2024.08.011
18. Eggermann T. Human reproduction and disturbed genomic imprinting. Genes (Basel). 2024; 26; 15(2): 163. https://dx.doi.org/10.3390/genes15020163
19. Zakar T., Paul J.W. Fetal membrane epigenetics. Front. Physiol. 2020; 11: 588539. https://dx.doi.org/10.3389/fphys.2020.588539
20. Zampieri F., Thiene G., Basso C., Zanatta A. The three fetal shunts: A story of wrong eponyms. J. Anat. 2021; 238(4): 1028-35. https://dx.doi.org/10.1111/joa.13357
21. Shi J.X., Yang L., Gan J., Gu W.W., Gu Y., Shi Y. et al. MiR-3074-5p regulates trophoblasts function via EIF2S1/GDF15 pathway in recurrent miscarriage. Reprod. Sci. 2024; 31(5): 1290-302. https://dx.doi.org/10.1007/s43032-023-01436-0
22. Jia Z., Wei Y., Zhang Y., Song K., Yuan J. Metabolic reprogramming and heterogeneity during the decidualization process of endometrial stromal cells. Cell Commun. Signal. 2024; 22(1): 385. https://dx.doi.org/10.1186/s12964-024-01763-y
23. Zhao Q.Y., Li Q.H., Fu Y.Y., Ren C.E., Jiang A.F., Meng Y.H. Decidual macrophages in recurrent spontaneous abortion. Front. Immunol. 2022; 13: 994888. https://dx.doi.org/10.3389/fimmu.2022.994888
24. Stevens D.U., de Nobrega Teixeira J.A., Spaanderman M.E.A., Bulten J., van Vugt J.M.G., Al-Nasiry S. Understanding decidual vasculopathy and the link to preeclampsia: A review. Placenta. 2020; 97: 95-100. https://dx.doi.org/10.1016/j.placenta.2020.06.020
25. Pantos K., Grigoriadis S., Maziotis E., Pistola K., Xystra P., Pantou A. et al. The role of interleukins in recurrent implantation failure: a comprehensive review ofthe literature. Int. J. Mol. Sci. 2022; 23(4): 2198. https://dx.doi.org/10.3390/ijms23042198
26. He Y., Ju Y., Lei H., Dong J., Jin N., Lu J. et al. MiR-135a-5p regulates window of implantation by suppressing pinopodes development and decidualization of endometrial stromal cells. J. Assist. Reprod. Genet. 2024; 41(6): 1645-59. https://dx.doi.org/10.1007/s10815-024-03088-8
27. Sun C., Groom K.M., Oyston C., Chamley L.W., Clark A.R., James J.L. The placenta in fetal growth restriction: What is going wrong? Placenta. 2020; 96: 10-8. https://dx.doi.org/10.1016/j.placenta.2020.05.003
28. Vondra S., Höbler A.L., Lackner A.I., Raffetseder J., Mihalic Z.N., Vogel A. et al. The human placenta shapes the phenotype of decidual macrophages. Cell Rep. 2023; 42(1): 111977. https://dx.doi.org/10.1016/j.celrep.2022.111977
29. Yousefzadeh Y., Soltani-Zangbar M.S., Kalafi L., Tarbiat A., Shahmohammadi Farid S., Aghebati-Maleki L. et al. Evaluation of CD39, CD73, HIF-1α, and their related miRNAs expression in decidua of preeclampsia cases compared to healthy pregnant women. Mol. Biol. Rep. 2022; 49(11): 10183-93. https://dx.doi.org/10.1007/s11033-022-07887-z
30. Zhou M., Xu H., Zhang D., Si C., Zhou X., Zhao H. et al. Decreased PIBF1/IL6/p-STAT3 during the mid-secretory phase inhibits human endometrial stromal cell proliferation and decidualization. J. Adv. Res. 2020; 30: 15-25. https://dx.doi.org/10.1016/j.jare.2020.09.002
31. Guo X., Yi H., Li T.C., Wang Y., Wang H., Chen X. Role of vascular endothelial growth factor (VEGF) in human embryo implantation: clinical implications. Biomolecules. 2021; 11(2): 253. https://dx.doi.org/10.3390/biom11020253
32. Тезиков Ю.В., Липатов И.С., Фролова Н.А., Кутузова О.А., Приходько А.В., Рябова С.А. Информативность предикторов больших акушерских синдромов у беременных с эмбриоплацентарной дисфункцией. Аспирантский вестник Поволжья. 2015; 5-6: 48-55.
33. Johnson G.A., Burghardt R.C., Bazer F.W., Seo H., Cain J.W. Integrins and their potential roles in mammalian pregnancy. J. Anim. Sci. Biotechnol. 2023; 14(1): 115. https://dx.doi.org/10.1186/s40104-023-00918-0
34. Flores-Espinosa P., Méndez I., Irles C., Olmos-Ortiz A., Helguera-Repetto C., Mancilla-Herrera I. et al. Immunomodulatory role of decidual prolactin on the human fetal membranes and placenta. Front. Immunol. 2023; 14: 1212736. https://dx.doi.org/10.3389/fimmu.2023.1212736
35. Kimura M., Kajihara T., Mizuno Y., Sato T., Ishihara O. Loss of high-mobility group N5 contributes to the promotion of human endometrial stromal cell decidualization. Reprod. Med. Biol. 2018; 17(4): 493-9. https://dx.doi.org/10.1002/rmb2.12226
36. Menkhorst E., So T., Rainczuk K., Barton S., Zhou W., Edgell T. et al. Endometrial stromal cell miR-19b-3p release is reduced during decidualization implying a role in decidual-trophoblast cross-talk. Front. Endocrinol. (Lausanne). 2023; 14: 1149786. https://dx.doi.org/10.3389/fendo.2023.1149786
37. Сухих Г.Т., Силачев Д.Н., Горюнов К.В., Волочаева М.В., Шмаков Р.Г. Роль дисфункции стволовых клеток в развитии больших акушерских синдромов. Акушерство и гинекология. 2018; 7: 5-11.
38. Низяева Н.В., Амирасланов Э.Ю., Ломова Н.А., Павлович С.В., Савельева Н.А., Наговицына М.Н., Сухачёва Т.В., Серов Р.А., Щеголев А.И., Kан Н.Е. Ультраструктурные и иммуногистохимические особенности плаценты при преэклампсии в сочетании с задержкой роста плода. Акушерство и гинекология. 2019; 11: 97-106. Nizyaeva N.V., Amiraslanov E.Yu., Lomova N.A., Pavlovich S.V., Savel’eva N.A., Nagovitsyna M.N., Sukhacheva T.V., Serov R.A., A.I. Shchegolev, Kan N.E. Placental ultrastructural and immunohistochemical changes in preeclampsia with concomitant fetal growth restriction. Obstetrics and Gynecology. 2019; (11): 97-106. (in Russian)]. https://dx.doi.org/10.18565/aig.2019.11.97-106
39. Garrido-Gomez T., Quiñonero A., Dominguez F., Rubert L., Perales A., Hajjar K.A. et al. Preeclampsia: a defect in decidualization is associated with deficiency of Annexin A2. Am. J. Obstet. Gynecol. 2020; 222(4): 376.e1-376.e17. https://dx.doi.org/10.1016/j.ajog.2019.11.1250
40. Lin X., Dai Y., Gu W., Zhang Y., Zhuo F., Zhao F. et al. The involvement of RNA N6-methyladenosine and histone methylation modification in decidualization and endometriosis-associated infertility. Clin. Transl. Med. 2024; 14(2): e1564. https://dx.doi.org/10.1002/ctm2.1564
41. Bonney E.A., Johnson M.R. The role of maternal T cell and macrophage activation in preterm birth: Cause or consequence? Placenta. 2019; 79: 53-61. https://dx.doi.org/10.1016/j.placenta.2019.03.003
42. Goto S., Ozaki Y., Ozawa F., Yoshihara H., Ujvari D., Kitaori T. et al. Impaired decidualization and relative increase of PROK1 expression in the decidua of patients with unexplained recurrent pregnancy loss showing insulin resistance. J. Reprod. Immunol. 2023; 160: 104155. https://dx.doi.org/10.1016/j.jri.2023.104155
43. Yang J., Li L., Wang L., Chen R., Yang X., Wu J. et al. Trophoblast-derived miR-410-5p induces M2 macrophage polarization and mediates immunotolerance at the fetal-maternal interface by targeting the STAT1 signaling pathway. J. Transl. Med. 2024; 22(1): 19 https://dx.doi.org/10.1186/s12967-023-04831-y
44. Lothert P.K., Fedyshyn B., Girard S., Chakraborty R., Norgan A.P., Enninga E.A.L. Spatial proteomics reveals phenotypic and functional differences in T cell and macrophage subsets during villitis of unknown etiology. Sci. Rep. 2024; 14(1): 914. https://dx.doi.org/10.1038/s41598-024-51545-2
45. Xu R., Li C., Liu X., Gao S. Insights into epigenetic patterns in mammalian early embryos. Protein Cell. 2021; 12(1): 7-28. https://dx.doi.org/10.1007/s13238-020-00757-z
46. Zhang Q., Tian P., Xu H. MicroRNA-155-5p regulates survival of human decidua stromal cells through NF-κB in recurrent miscarriage. Reprod. Biol. 2021; 21(3): 100510. https://dx.doi.org/10.1016/j.repbio.2021.100510
47. Липатов И.С., Тезиков Ю.В., Мартынова Н.В., Мингалиева Л.К., Гогель Л.Ю., Белоконева Т.С., Калинкина О.Б., Жернакова Е.В., Юсупова Р.Р. Универсальный подход к профилактике синдрома патологической беременности. Наука и инновации в медицине. 2017; 1(5): 13-23.
48. Dai W., Guo R., Na X., Jiang S., Liang J., Guo C. et al. Hypoxia and the endometrium: An indispensable role for HIF-1α as therapeutic strategies. Redox. Biol. 2024; 73: 103205. https://dx.doi.org/10.1016/j.redox.2024.103205
49. Muneeba S. Jr., Acharya N., Mohammad S. The role of dydrogesterone in the management of luteal phase defect: a comprehensive review. Cureus. 2023; 15(11): e48194. https://dx.doi.org/10.7759/cureus.48194
50. Yuan L., Wu H., Huang W., Bi Y., Qin A., Yang Y. The function of metformin in endometrial receptivity (ER) of patients with polycyclic ovary syndrome (PCOS): a systematic review and meta-analysis. Reprod. Biol. Endocrinol. 2021; 19(1): 89. https://dx.doi.org/10.1186/s12958-021-00772-7
51. Lasch M., Sudan K., Paul C., Schulz C., Kolben T., Dorp J.V. et al. Isolation of decidual macrophages and hofbauer cells from term placenta-comparison of the expression of CD163 and CD80. Int. J. Mol. Sci. 2022; 23(11): 6113. https://dx.doi.org/10.3390/ijms23116113
52. Zong Y., Wang X., Wang J. Research progress on the correlation between gut microbiota and preeclampsia: microbiome changes, mechanisms and treatments. Front. Cell Infect. Microbiol. 2023; 13: 1256940. https://dx.doi.org/10.3389/fcimb.2023.1256940
53. Li P., Wang H., Guo L., Gou X., Chen G., Lin D. et al. Association between gut microbiota and preeclampsia-eclampsia: a two-sample Mendelian randomization study. BMC Med. 2022; 20(1): 443. https://dx.doi.org/10.1186/s12916-022-02657-x
54. Chaemsaithong P., Sahota D.S., Poon L.C. First trimester preeclampsia screening and prediction. Am. J. Obstet. Gynecol. 2022; 226(2S): S1071-S1097.e2. https://dx.doi.org/10.1016/j.ajog.2020.07.020
55. Rong M., Yan X., Zhang H., Zhou C., Zhang C. Dysfunction of decidual macrophages is a potential risk factor in the occurrence of preeclampsia. Front. Immunol. 2021; 12(12): 655655. https://dx.doi.org/10.3389/fimmu.2021.655655
56. Smith D.D., Costantine M.M. The role of statins in the prevention of preeclampsia. Am. J. Obstet. Gynecol. 2022; 226(2S): S1171-S1181. https://dx.doi.org/10.1016/j.ajog.2020.08.040
57. Statins: Drug Safety Communication – FDA Requests Removal of Strongest Warning Against Using Cholesterol-lowering Statins During Pregnancy. Available at: https://www.fda.gov/safety/medical-product-safety-information/statins-drug-safety-communication-fda-requests-removal-strongest-warning-against-using-cholesterol
58. Chang J., Chen Y., Chen I., Lin W., Chen Y., Lin C. Perinatal outcomes after statin exposure during pregnancy. JAMA Netw. Open. 2021; 4(12): e2141321. https://dx.doi.org/10.1001/jamanetworkopen.2021.41321
59. Борис Д.А., Тютюнник В.Л., Кан Н.Е., Щеголев А.И., Синицына В.А., Садекова А.А., Красный А.М. Особенности изменения клеток моноцитарно-макрофагального звена в плаценте при преэклампсии. Акушерство и гинекология. 2021; 10: 48-54.
60. Erez O., Romero R., Jung E., Chaemsaithong P., Bosco M., Suksai M. et al. Preeclampsia and eclampsia: the conceptual evolution of a syndrome. Am. J. Obstet. Gynecol. 2022; 226(2S): S786-S803. https://dx.doi.org/10.1016/j.ajog.2021.12.001

Поступила 23.12.2024

Принята в печать 18.04.2025